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Home > Active Pharmaceutical Ingredients > Antibiotics > Cefotaxime sodium for Sale > Cefotaxime Sodium CAS 64485-93-4 High Purity Factory Direct Supply Fast Delivery Professional After-Sale
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Cefotaxime Sodium CAS 64485-93-4 High Purity Factory Direct Supply Fast Delivery Professional After-Sale

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Unit Price: Get Latest Price
CAS No.:

64485-93-4

Grade:

Pharmaceutical Grade

Content:

99%

Port:

Shanghai

Brand:

WANWEI

Packaging:

25kg/Cardboard Drum

Price valid (until):

2026-06-18

Company Type:
Trader
Location:
China
Qualification:
Main Products:

Tirzepatide,Retatrutide,Semaglutide

  • Product Description

  • Seller Information

  • Inquiry History

  • Description


      Product Detail  


    *Product Photos

    Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 1 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 2 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 3 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 4 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 5 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 6 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 7 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 8 Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 9

    Product Introduction

    Item Cefotaxime Sodium
    Cas No. 64485-93-4
    Purity >99

    1. Product Overview


    Cefotaxime Sodium is a representative third-generation semi-synthetic cephalosporin antibiotic, with the chemical name (6R,7R)-3-[(Acetoxy)methyl]-7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt. Its molecular formula is C₁₆H₁₈N₅NaO₇S₂ and molecular weight is 479.46.

    The product appears as white, off-white or pale yellow crystalline powder, odorless or slightly having a special odor, with significant hygroscopicity and easy moisture absorption when exposed to air. As a Class A national medical insurance prescription drug and an essential medicine listed in the WHO Essential Medicines List, it is one of the core drugs for clinical anti-infective treatment worldwide.

    Cefotaxime Sodium is prepared through chemical synthesis, using 7-aminocephalosporanic acid (7-ACA) as the mother nucleus and introducing a methoxyimino thiazole acetyl side chain. This structural design endows it with high stability against β-lactamases produced by Gram-negative bacteria, solving the defect that early cephalosporins are easily degraded by enzymes. Its purity is not less than 96.0% as determined by high-performance liquid chromatography (HPLC) and nonaqueous titration, complying with international authoritative standards such as the United States Pharmacopeia (USP), European Pharmacopoeia (EP), British Pharmacopoeia (BP), and Chinese Pharmacopoeia (ChP).

    In the global pharmaceutical market, relying on its broad-spectrum antibacterial activity, excellent tissue penetration, and good safety profile, Cefotaxime Sodium is widely used in the treatment of moderate to severe infections caused by susceptible bacteria in hospitalized patients. It holds an irreplaceable clinical position especially in the treatment of severe infections such as pediatric meningitis and sepsis.

    2. Mechanism of Action & Functional Activity


    2.1 Antibacterial Mechanism


    Cefotaxime Sodium exerts its antibacterial effect by binding to penicillin-binding proteins (PBPs) on the bacterial cell membrane, inhibiting the peptidoglycan cross-linking reaction in the bacterial cell wall. This leads to defective cell wall synthesis and reduced mechanical strength, causing bacterial cells to swell, rupture, and die under osmotic pressure. The methoxyimino structure in its side chain can effectively shield the attack site of β-lactamases, significantly enhancing stability against β-lactamases produced by Gram-negative bacteria, and its antibacterial spectrum is far superior to that of first and second-generation cephalosporins.

    2.2 Antibacterial Activity


    • Susceptible Bacteria: It exhibits strong activity against Enterobacteriaceae (Escherichia coli, Klebsiella spp., Salmonella spp., Shigella spp., etc.), with MIC₉₀ values mostly ranging from 0.03 to 0.5μg/ml; it has extremely low MIC₉₀ values (0.015-0.06μg/ml) against Haemophilus influenzae (including β-lactamase-producing strains) and Neisseria meningitidis; for Gram-positive cocci such as Streptococcus pneumoniae and Streptococcus pyogenes, the MIC₉₀ values are 0.015-0.12μg/ml.
    • Weakly Active/Resistant Bacteria: It shows moderate activity against methicillin-susceptible Staphylococcus aureus (MIC₉₀=1-4μg/ml), no antibacterial activity against Pseudomonas aeruginosa and Alcaligenes spp., and complete resistance to methicillin-resistant Staphylococcus aureus (MRSA) and Enterococcus spp.

    3. Clinical Significance & Applications


    3.1 Clinical Value


    With its broad-spectrum antibacterial activity, excellent tissue penetration, and good safety profile, Cefotaxime Sodium has become a first-line drug for the treatment of moderate to severe infections caused by susceptible bacteria. It can quickly reach effective blood concentration and penetrate the blood-brain barrier, with cerebrospinal fluid concentration accounting for 10%-20% of serum concentration, making it one of the important therapeutic drugs for bacterial meningitis in adults and children.

    In addition, the drug has unique advantages in the treatment of newborn infections. With low nephrotoxicity, it can be safely adjusted according to body weight and is widely used in the treatment of sepsis and meningitis in premature infants and full-term newborns.

    3.2 Main Application Areas


    • Respiratory Tract Infections: Treatment of community-acquired pneumonia, hospital-acquired pneumonia, lung abscess, bronchiectasis with infection, etc., especially suitable for critically ill patients with concurrent sepsis or respiratory failure.
    • Central Nervous System Infections: Treatment of bacterial meningitis caused by Haemophilus influenzae, Neisseria meningitidis, Streptococcus pneumoniae, Escherichia coli, etc., and it is one of the first-choice drugs for pediatric meningitis.
    • Urinary Tract Infections: Used for acute pyelonephritis, complicated urinary tract infections (such as those associated with urinary tract obstruction or catheter-related infections). The drug has high concentration in kidney tissue and can effectively eliminate pathogenic bacteria in lesions.
    • Sepsis & Bloodstream Infections: As a core drug for the treatment of sepsis caused by Gram-positive and negative bacteria, it can quickly control bacterial proliferation in the bloodstream and reduce the risk of septic shock.
    • Abdominal & Pelvic Infections: Used for peritonitis, cholangitis, cholecystitis, intra-abdominal abscess, pelvic inflammatory disease, endometritis, etc., often combined with anti-anaerobic drugs such as metronidazole.
    • Skin & Soft Tissue Infections: Treatment of cellulitis, erysipelas, wound infections, burn infections, etc., which can effectively control local inflammation and prevent infection from spreading to deep tissues.
    • Bone & Joint Infections: Used for osteomyelitis and suppurative arthritis. The drug can penetrate bone tissue and synovial fluid to reach effective antibacterial concentration.

    4. Storage & Handling


    4.1 Storage Conditions


    • Temperature: Should be stored in a refrigerated environment at 2-8℃, avoiding exposure to high temperatures above 30℃. High temperatures will accelerate the hydrolysis of the β-lactam ring and lead to a decrease in drug potency.
    • Humidity: The relative humidity of the storage environment should be controlled at 30%-60% to prevent the product from absorbing moisture and caking, which may affect solubility and stability.
    • Light Protection: Use opaque packaging containers (such as aluminum foil composite bags, amber glass bottles) to avoid photodegradation reactions caused by ultraviolet radiation.
    • Atmosphere: It is recommended to store under the protection of inert gases to reduce the oxidation of the drug by oxygen in the air.

    4.2 Packaging Specifications


    Customizable according to customer requirements.

    4.3 Shelf Life & Handling Precautions


    • Shelf Life: Under the recommended sealed, refrigerated and light-protected storage conditions, the shelf life is 24 months from the date of manufacture. The potency of expired products may decrease significantly, and the content of related impurities may exceed the limit, so they are strictly prohibited from use.
    • Handling Precautions: The product should be used within 24 hours after opening the package. If not used immediately, it should be resealed tightly and stored in a refrigerator for a maximum of 72 hours. During transportation, refrigerated trucks or insulated containers with ice packs should be used to maintain the temperature at 2-8℃, avoiding violent shock, collision, exposure to sunlight and rain. Unused or expired products and packaging materials are classified as pharmaceutical waste, which should be handled by professional institutions in accordance with local environmental protection regulations to avoid environmental pollution.

    Shop N-Ethyl-3-cyano-4-methyl-6-hydroxy-2-pyridone CAS 29097-12-9 Factory Direct Supply High Quality Low Price-Detailed Image 10

    Certificates
    • Cefotaxime Sodium CAS 64485-93-4 High Purity Factory Direct Supply Fast Delivery Professional After-Sale Certificates 1

    Basic Info
    Product Name:

    Cefotaxime sodium

    Other Name:

    5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[(acetyloxy)methyl]-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-,sodium salt (1:1),(6R,7R)-;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[(acetyloxy)methyl]-7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-,monosodium salt,[6R-[6α,7β(Z)]]-;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[(acetyloxy)methyl]-7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-,monosodium salt,(6R,7R)-;HR 756;RU 24756;Cefotaxime sodium salt;Cefotaxime sodium;(+)-Cefotaxime sodium salt;Tolycar;Sodium cefotaxime;Chemcef;Pretor;Cefotax;Oritaxim;Biotax;Cefantral;Novatax;Cefomerc;Sefagen;Clafora;Baxim;Biolog;Bioxim;CefSo;Cefacron;Cefcan;Cefomed;Cefomerk;Cefon;Cefotam;Cefoxim;Ceftim;Ceftop;Ceftoringe;Cefronate;Calcef;Claftax;Clavox;Califrid;Eaxiron;Elkotak;Epotazime;Evotaxime;Excef;Forax;Fortax;Zafixime

    CAS No.:

    64485-93-4

    Molecular Formula:

    C16H17N5O7S2.Na

    InChIKeys:

    InChIKey=UWNYOXHAYFLGIE-JUZDKLSSSA-N

    Molecular Weight:

    477.45

    EC Number:

    264-915-9

    HScode:

    29419000

    Categories:

    Antibiotics

    Characteristics
    PSA:

    229.88000

    XLogP3:

    -1.04720

    Appearance:

    white to yellow powder

    Density:

    1.8 g/cm3

    Melting Point:

    162-163 C

    Water Solubility:

    soluble in water.H2O: aqueous solutions of pH 4.3-6.2 are stable up to 3 weeks at 2-8 °C.soluble

    Storage Conditions:

    2-8°C

    Toxicity:

    Oral-rat LD50: > 20000 mg/kg; Oral-Mouse LD50: > 20000 mg/kg

    Flammability characteristics:

    Thermal decomposition releases toxic nitrogen oxides, sulfur oxides, sodium oxide fumes

    Specific rotation:

    D20 +55±2° (c = 0.8 in water)

    Hazard Identification

    Classification of the substance or mixture

    Skin sensitization, Category 1

    Respiratory sensitization, Category 1

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Danger

    Hazard statement(s)

    H317 May cause an allergic skin reaction

    H334 May cause allergy or asthma symptoms or breathing difficulties if inhaled

    Precautionary statement(s)
    Prevention

    P261 Avoid breathing dust/fume/gas/mist/vapours/spray.

    P272 Contaminated work clothing should not be allowed out of the workplace.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    P284 [In case of inadequate ventilation] wear respiratory protection.

    Response

    P302+P352 IF ON SKIN: Wash with plenty of water/...

    P333+P317 If skin irritation or rash occurs: Get medical help.

    P321 Specific treatment (see ... on this label).

    P362+P364 Take off contaminated clothing and wash it before reuse.

    P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.

    P342+P316 If experiencing respiratory symptoms: Get emergency medical help immediately.

    Storage

    none

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Trader

    Main Products:

    Tirzepatide,Retatrutide,Semaglutide

    Location:

    No. 2302, Changqing Road, Gaoyuan Community, Laodaohe Sub-district, Kaifu District, Changsha City, Hunan Province

    Payment Terms:

    TT against copy of documents,D/P,L/C,D/A,TT against B/L draft before shipment,100% TT in advance

    Average lead Time:

    10

    Total Annual Revenue:

    $10 million-$25 million

    Total Employees:

    101-200

    Year of Establishment:

    2023

    Changsha Wanwei Technology Co., Ltd. has been deeply engaged in the biopharmaceutical industry for over 20 years and stands as a global leader in the metabolic disease drug sector. Leveraging its integrated end-to-end capabilities covering "R&D, production, and commercialization" as well as profound industry expertise, the company firmly ranks among the top tier of the global biopharmaceutical industry. Its core products include multiple key varieties such as Semaglutide, Tirzepatide, Retatrutide, and Cagrilintide.​
    Eighty percent of the members in the company's core team possess over 15 years of experience in metabolic drug R&D. Many of them have led the launch of internationally blockbuster antidiabetic drugs. The team has successfully facilitated the approval of 12 innovative drugs, among which 5 have become top 50 best-selling prescription drugs globally. This has enabled the company to establish an irreplicable technical and experiential barrier in fields such as peptide drug molecular modification and long-acting formulation development.​
    On the R&D front, the company has built four national-level technology platforms, including peptide molecular design and oral formulation innovation, and holds more than 300 authorized patents. Its drug R&D cycle is 30% shorter than the industry average. On the production side, it owns the world's largest intelligent base for peptide drugs, with an annual production capacity of 500 kilograms. The base complies with the triple GMP standards of China, the United States, and the European Union, and achieves a 90% self-sufficiency rate in key raw materials, ensuring stable supply to over 120 countries. Additionally, the company has passed the unannounced inspections by the FDA (U.S. Food and Drug Administration) and EMA (European Medicines Agency) for 10 consecutive years.​
    Currently, Semaglutide has overcome the challenge of low oral bioavailability, achieving global sales of over 15 billion US dollars within 3 years of its launch. Tirzepatide surpassed 8 billion US dollars in sales in its first year on the market. Retatrutide has entered Phase III clinical trials, while the combination therapy of Cagrilintide is in Phase II clinical development. All these products demonstrate revolutionary therapeutic value. Looking ahead, the company will invest 25% of its annual revenue in R&D, focusing on the fields of metabolism and cardiovascular diseases, and is committed to becoming a global innovation benchmark in the biopharmaceutical industry.

  • Inquiry History
    3 Inquiries
    Country Product Purchase Quantity Date Posted
    Egypt

    Cefotaxime sodium, CEFOTAXIME SODIUM 98% white powder 64485-93-4 Senwayer

    5 KG May 27, 2024
    Egypt

    Cefotaxime Sodium

    10.00 KG Sep 20, 2023
    India

    CEFOTAXIME SODIUM

    105 KG Feb 5, 2025
    Post an enquiry for this product
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